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139057-06-0

5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 139057-06-0 Structure

  • Basic information

    1. Product Name: 5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone
    2. Synonyms: 5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone
    3. CAS NO:139057-06-0
    4. Molecular Formula: C17H19N3O3
    5. Molecular Weight: 313.35106
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 139057-06-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone(139057-06-0)
    11. EPA Substance Registry System: 5-acetyl-6-methyl-4-(4-morpholinyl)-1-phenyl-2(1H)-pyrimidinone(139057-06-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 139057-06-0(Hazardous Substances Data)

139057-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139057-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,5 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139057-06:
(8*1)+(7*3)+(6*9)+(5*0)+(4*5)+(3*7)+(2*0)+(1*6)=130
130 % 10 = 0
So 139057-06-0 is a valid CAS Registry Number.

139057-06-0Downstream Products

139057-06-0Relevant articles and documents

COMPOUNDS FOR IMMUNOPOTENTIATION

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Page/Page column 150, (2010/02/15)

Methods of stimulating an immune response and treating patients responsive thereto with 3,4-di(1H-indol-3-yl)-1H-pyrrole-2,5-diones, staurosporine analogs, derivatized pyridazines, chromen-4-ones, indolinones, quinazolines, nucleoside analogs, and other small molecules are disclosed.

SYNTHESIS OF DERIVATIVES OF 4-ALKYLTHIOURACIL, CYTOSINE, PYRIDOPYRIMIDINE, AND PYRIMIDOPYRIMIDINE FROM THE N,S- AND N,N-ACETALS OF DIACETYLKETENE AND ISOCYANATES

Dorokhov, V.A.,Gordeev, M.F.,Komkov, A.V.,Bogdanov, V.S.

, p. 2267 - 2273 (2007/10/02)

The action of alkyl and aryl isocyanates on the N,S-acetals of diacetylketene leads to the formation of 4-alkylthio-5-acetyl-1-alkyl(aryl)-6-methyl-1H-pyrimidin-2-ones (derivatives of 4-alkylthiouracils).The reaction of the synthesized thiouracils with am

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